Evidence map›Paper›PMID 36547390›Full record

ArticleImmunoHorizons2022

Dam-Infant Rhesus Macaque Pairs to Dissect Age-Dependent Responses to SARS-CoV-2 Infection.

Stephanie N Langel, Carolina Garrido, Caroline Phan, Tatianna Travieso, Helene Kirshner, Todd DeMarco, Zhong-Min Ma, J Rachel Reader, Katherine J Olstad, Rebecca L Sammak and 11 more

Open access · goldAbstract read
In one paragraph

Article in ImmunoHorizons, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 1 country.

Stephanie N LangelCenter for Global Health and Diseases, Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH.
Carolina GarridoDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC.
Caroline PhanDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC.
Tatianna TraviesoDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC.
Helene KirshnerDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC.ORCID 0000-0003-4110-0983
Todd DeMarcoDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC.
Zhong-Min MaCalifornia National Primate Research Center, University of California, Davis, Davis, CA.ORCID 0000-0003-3713-7337
J Rachel ReaderCalifornia National Primate Research Center, University of California, Davis, Davis, CA.
Katherine J OlstadCalifornia National Primate Research Center, University of California, Davis, Davis, CA.ORCID 0000-0003-3894-0981
Rebecca L SammakCalifornia National Primate Research Center, University of California, Davis, Davis, CA.ORCID 0000-0003-3271-0413
Yashavanth Shaan LakshmanappaCenter for Immunology and Infectious Diseases, University of California, Davis, Davis, CA.
Jamin W RohCenter for Immunology and Infectious Diseases, University of California, Davis, Davis, CA.
Jennifer WatanabeCalifornia National Primate Research Center, University of California, Davis, Davis, CA.ORCID 0000-0001-9408-3991
Jodie UsachenkoCalifornia National Primate Research Center, University of California, Davis, Davis, CA.
Ramya ImmareddyCalifornia National Primate Research Center, University of California, Davis, Davis, CA.
Rachel PollardCenter for Immunology and Infectious Diseases, University of California, Davis, Davis, CA.
Smita S IyerCalifornia National Primate Research Center, University of California, Davis, Davis, CA.
Sallie PermarDepartment of Pediatrics, New York-Presbyterian Hospital/Weill Cornell Medical Center, New York, NY; and.
Lisa A MillerCalifornia National Primate Research Center, University of California, Davis, Davis, CA.ORCID 0000-0001-7557-1316
Koen K A Van RompayCalifornia National Primate Research Center, University of California, Davis, Davis, CA.ORCID 0000-0002-7375-1337
Maria BlasiDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC.ORCID 0000-0002-7091-0312
University of California, Davis · USDuke University · USCenter for Global Health · USNewYork–Presbyterian Hospital · US

Funding

National Institute on Aging (NIA) ColonyP51OD011107 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Simon J. Atkinson · 2012 to 2026
$191.5M
Regional Biocontainment Laboratory (RBL)UC6AI058607 · NIAID · DUKE UNIVERSITY · PI WILLIAMS, R SANDERS · 2003 to 2005
$16.3M
Regional Biocontainment Laboratories Facility and Building System Upgrades SupportG20AI167200 · NIAID · DUKE UNIVERSITY · PI STAATS, HERMAN F · 2021 to 2022
$6.6M
NIAID NIH HHS G20 AI167200NIAID NIH HHS HHSN272201800003CNIAID NIH HHS UC6 AI058607NIH HHS P51 OD011107
6 · The paper itself

Abstract

The global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its associated coronavirus disease (COVID-19) has led to a pandemic of unprecedented scale. An intriguing feature of the infection is the minimal disease in most children, a demographic at higher risk for other respiratory viral diseases. To investigate age-dependent effects of SARS-CoV-2 pathogenesis, we inoculated two rhesus macaque monkey dam-infant pairs with SARS-CoV-2 and conducted virological and transcriptomic analyses of the respiratory tract and evaluated systemic cytokine and Ab responses. Viral RNA levels in all sampled mucosal secretions were comparable across dam-infant pairs in the respiratory tract. Despite comparable viral loads, adult macaques showed higher IL-6 in serum at day 1 postinfection whereas CXCL10 was induced in all animals. Both groups mounted neutralizing Ab responses, with infants showing a more rapid induction at day 7. Transcriptome analysis of tracheal airway cells isolated at day 14 postinfection revealed significant upregulation of multiple IFN-stimulated genes in infants compared with adults. In contrast, a profibrotic transcriptomic signature with genes associated with cilia structure and function, extracellular matrix composition and metabolism, coagulation, angiogenesis, and hypoxia was induced in adults compared with infants. Our study in rhesus macaque monkey dam-infant pairs suggests age-dependent differential airway responses to SARS-CoV-2 infection and describes a model that can be used to investigate SARS-CoV-2 pathogenesis between infants and adults.

Indexed as

COVID-19AnimalsLungMacaca mulattaSARS-CoV-2Virus Replication

Identifiers

PMID36547390
PMCPMC10538284
OpenAlexW4312211883

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.